Evidence map›Paper›PMID 30076402›Full record

ReviewJournal of perinatology : official journal of the California Perinatal Association2018

Peri-mortem evaluation of infants who die without a diagnosis: focus on advances in genomic technology.

Monica H Wojcik, Dara Brodsky, Jane E Stewart, Jonathan Picker

Open access · greenAbstract readReview
In one paragraph

Review in Journal of perinatology : official journal of the California Perinatal Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Infant mortality: the contribution of genetic disorders.Journal of perinatology : official journal of the California Perinatal Association · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Monica H WojcikDivision of Newborn Medicine, Department of Medicine, Boston Children's Hospital, Boston, MA, USA. monica.wojcik@childrens.harvard.edu.ORCID 0000-0002-8162-5031
Dara BrodskyDepartment of Neonatology, Beth Israel Deaconness Medical Center, Boston, MA, USA.
Jane E StewartDepartment of Neonatology, Beth Israel Deaconness Medical Center, Boston, MA, USA.
Jonathan PickerDivision of Genetics and Genomics, Department of Medicine, Boston Children's Hospital, Boston, MA, USA.
Beth Israel Deaconess Medical Center · USBoston Children's Hospital · US

Funding

TRAINING GRANT IN GENETICST32GM007748 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI Anne O'Donnell-Luria, Louise Wilkins-Haug · 1985 to 2026
$12.0M
NIGMS NIH HHS T32 GM007748U.S. Department of Health & Human Services | National Institutes of Health (NIH) T32GM007748
6 · The paper itself

Abstract

Infants who die within the first weeks to months of life may have genetic disorders, though many die without a confirmed diagnosis. Non-genetic conditions may also be responsible for unexplained infant deaths, and the diagnosis may be reliant upon studies performed in the peri-mortem period. Neonatologists, obstetricians, or pediatricians caring for these children and their families may be unsure of which investigations can and should be performed in the setting of a newborn or infant who is dying or has died. Recent advances in genomic sequencing technology may provide additional diagnostic options, though the interpretation of genetic variants discovered by this technique may be contingent upon clinical phenotype information that is obtained peri-mortem or upon autopsy. We have reviewed the current literature concerning the evaluation of an unexplained neonatal or infantile demise and synthesized a diagnostic approach, with a focus on the contribution of new and emerging genomic technologies.

Indexed as

AutopsyGenomicsHumansInfantInfant DeathInfant, NewbornSudden Infant Death

Identifiers

PMID30076402
PMCPMC6419510
OpenAlexW2886678889

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.